Dendritic cells having enhanced yo t-cell activating and/or proliferating activity and methods of preparation or use thereof

ABSTRACT

A therapeutic method, which includes administering dendritic cells pulsed in vitro with a bisphosphonate-based bone metabolism improving drug, is provided. The dendritic cells may be capable of efficiently activating and/or proliferating γδ T-cells in vivo and/or in vitro. This can permit for easy proliferation of γδ T-cells without burdening a patient, leading to practical applications of immune cell therapies that utilize γδ T-cells.

CROSS REFERENCE TO RELATED APPLICATIONS

This patent application is a divisional of U.S. patent application Ser.No. 11/631,660, which is a U.S. national stage of International PatentApplication PCT/JP2005/012971, filed on Jul. 7, 2005, which claims thebenefit and priority of Japanese Patent Application 2004-229991, filedon Jul. 8, 2004; the entire contents of these applications are herebyincorporated by reference in their entirety, for any and all purposes.

BACKGROUND

Dendritic cells work as antigen-presenting cells to present antigens,through phagocytosis and fragmentation, as antigenic epitopes on MajorHistocompatibility Complex (MHC) molecules at their cell surface. Whendendritic cells come in contact with T-cells in a lymph node, theT-cells recognize these antigenic epitopes.

In T-cells, αβ T-cells expressing αβ T-cell receptors and γδ T-cellsexpressing γδ T-cell receptors are present. The αβ T-cells primarilyassume the responsibility for acquired immunity, while the γδ T-cellswork as effector cells for immune responses to particular bacterialinfections such as tuberculosis, as well as tumors, and mainly assumethe responsibility for natural immunity.

It has recently been found that γδ T-cells also have cytotoxic activityagainst cancer cells, drawing attention to the development ofimmunotherapy utilizing the powerful antitumor activity possessed by γδT-cells. The vast majority of T-cells generally present in blood,however, are αβ T-cells; γδ T-cells account for a mere 1-5%.Accordingly, as a method to proliferate γδ T-cells, the γδ T-cells thatare separated using magnets and the like are cultured in vitro andreturned to the body.

It is known that γδ T-cells are also activated and/or proliferated bynonpeptide antigens; they are known to be activated and/or proliferatedby alkaloids such as alkylamines, as well as pyrophosphate monoestersand bisphosphonates.

Above all, methods to cultivate γδ T-cells in vitro utilizingbisphosphonates have been considered in various studies, but failed toproduce sufficient numbers of γδ T-cells. An attempt to obtain asufficient number of γδ T-cells suitable for a treatment meant anincrease in the amount of blood collected from a patient, which alsoincreased the burden placed on the patient. Accordingly, there exists aneed to establish a technique to easily obtain a sufficient number of γδT-cells not only in vitro, but also in vivo.

SUMMARY

The present application relates to dendritic cells pulsed withbisphosphonate-based bone metabolism improving drugs (hereinafterreferred to as bisphosphonates). The present application also relates topharmaceutical compositions comprising said dendritic cells, therapeuticmethods and γδ T-cell culture methods utilizing said dendritic cells.

The present application provides dendritic cells capable of efficientlyactivating and/or proliferating γδ T-cells in vivo and/or in vitro,pharmaceutical compositions comprising said dendritic cells, therapeuticmethods of the pharmaceutical compositions and γδ T-cell culture methodsutilizing said dendritic cells.

As a result of research in solving the aforementioned problems, theinventors found that γδ T-cells can be activated and/or proliferated byusing dendritic cells, which are normally used for CTL induction, pulsedwith bisphosphonates, instead of directly stimulating γδ T-cells withbisphosphonates. Furthermore, the inventors found that, unlike the caseof inducing antigen-specific αβ T-cells using a disease antigen peptide,γδ T-cells, unexpectedly, can be suitably activated and/or proliferatedby utilizing immature dendritic cells.

The present application enables easy proliferation of γδ T-cells withoutimposing a burden on a patient, leading to practical applications ofimmune cell therapies that utilize γδ T-cells.

The present application may achieve one or more of these objectives asdescribed below.

-   -   (1) Dendritic cells having been pulsed with a bisphosphonate;    -   (2) The dendritic cells of said (1), wherein said dendritic        cells are immature dendritic cells;    -   (3) The dendritic cells of said (1) or (2), wherein said        bisphosphonate is any one of pamidronic acid, alendronic acid,        zoledronic acid, risedronic acid, ibandronic acid, incadronic        acid, etidronic acid, their salts and/or their hydrates;    -   (4) A pharmaceutical composition comprising dendritic cells        pulsed with a bisphosphonate;    -   (5) The pharmaceutical composition of said (4), wherein said        dendritic cells are immature dendritic cells;    -   (6) The pharmaceutical composition of said (4) or (5), wherein        said bisphosphonate is any one of pamidronic acid, alendronic        acid, zoledronic acid, risedronic acid, ibandronic acid,        incadronic acid, etidronic acid, their salts and/or their        hydrates;    -   (7) A therapeutic method wherein dendritic cells pulsed with a        bisphosphonate are administered;    -   (8) The therapeutic method of said (7), wherein said dendritic        cells are immature dendritic cells;    -   (9) The therapeutic method of said (7) or (8), wherein said        bisphosphonate is any one of pamidronic acid, alendronic acid,        zoledronic acid, risedronic acid, ibandronic acid, incadronic        acid, etidronic acid, their salts and/or their hydrates;    -   (10) The therapeutic method of any of said (7) (9), wherein the        therapy is for treating cancers and/or infectious diseases;    -   (11) The therapeutic method of any of said (7) (11) [sic],        wherein said dendritic cells are autologous;    -   (12) A γδ T-cell culture method wherein dendritic cells pulsed        with a bisphosphonate are added;    -   (13) The γδ T-cell culture method of said (12), wherein said        dendritic cells are immature dendritic cells; and    -   (14) The γδ T-cell culture method of said (12) or (13), wherein        said bisphosphonate is any one of pamidronic acid, alendronic        acid, zoledronic acid, risedronic acid, ibandronic acid,        incadronic acid, etidronic acid, their salts and/or their        hydrates.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows the results of Example 3. Controls (dendritic cells notpulsed with a bisphosphonate), dendritic cells pulsed with Aredia,Onclast, and Zometa were respectively cocultivated with the reactedcells. The number of cells measured seven days later using ahemocytometer; the proportion of γδ T-cells measured using a flowcytometer; and the number of γδ T-cells calculated from the two figuresare shown.

FIG. 2 shows the results of Example 5. The ordinate indicates the numberof spots and the abscissa indicates the intensity of the spots. Asnegative controls, the IFN-γ produced by γδ T-cells alone; γδ T-cellsand Aredia; and the dendritic cells alone are shown.

DETAILED DESCRIPTION First Embodiment Preparation of the Dendritic Cells

The dendritic cells produced by the present methods will be explained indetail first.

The dendritic cells of the present application refer to dendritic cellshaving been pulsed with a bisphosphonate.

As the dendritic cells of the application, immature dendritic cells,mature dendritic cells, or the mixture of the two may be used. It ispreferable, however, to use immature dendritic cells, since they arecapable of more suitably activating and/or proliferating γδ T-cells.

Moreover, any bisphosphonate may be used as long as it functions as abone-resorption inhibitor and is generally used as a drug to treatosteoporosis. Examples include pamidronic acid, a salt thereof and/ortheir hydrates (for example, pamidronate disodium pentahydrate (Arediaby Novartis Pharma)), alendronic acid, a salt thereof and/or theirhydrates (for example, alendronate sodium trihydrate (Onclast by BanyuPharmaceutical)), zoledronic acid, a salt thereof and/or their hydrates(for example, zoledronate sodium hydrate (Zometa by Novartis Pharma)),risedronic acid, a salt thereof and/or their hydrates (for example,risedronate sodium hydrate), ibandronic acid, a salt thereof and/ortheir hydrates (for example, ibandronate sodium), incadronic acid, asalt thereof and/or their hydrates (for example, incadronate disodium),etidronic acid, a salt thereof and/or their hydrates (for example,etidronate disodium). Above all, pamidronic acid, alendronic acid,zoledronic acid, their salts and/or their hydrates are particularlypreferable.

Next, the method of preparing the dendritic cells of the presentapplication will be explained in detail.

A sample is obtained first in order to obtain precursors of dendriticcells. Peripheral blood, bone marrow, umbilical cord blood or the likecan be used as a sample. Considering the ease of collection and theminimal burden imposed on the patient, utilizing peripheral blood ispreferable.

It is preferable to collect an amount of blood that does not burden thedonor. As a method of collection, whole blood can be collected utilizinga vacuum blood tube or the like. Heparin or citric acid may be added sothat the collected blood does not coagulate. In the case wherein a largenumber of cells is required, peripheral blood monocytes can be directlyobtained by a method to collect the mononuclear component using acomponent collection system.

Mononuclear cells, or the precursors of dendritic cells, are thenseparated from the blood collected. Any method for separating nucleatedcells from red blood cells may be used. For example, the Ficollseparation method, i.e., a Ficoll-Paque density gradient, or elution iscommonly used.

In order to remove platelets and the like, it is preferable to clean thecollected cells several times using a culture medium, physiologicalsaline, phosphate buffered saline (hereinafter referred to as PBS) orthe like.

Next, the dendritic cell precursors are separated from the mononuclearcells collected.

Since CD14 is a known marker expressed in the dendritic cell precursors,a method to isolate and collect monocytes (CD14-positive cells)utilizing the Magnetic Cell Sorting (Miltenyi Biotec; hereinafterreferred to as MACS) is preferred since it is simple, and yields a highcell collection rate.

Another method may also be used, wherein the mononuclear cells collectedare cultivated for at least one hour in a culture flask under theconditions of 34-38° C., more preferably 37° C., and 2-10% CO2, morepreferably 5% CO2, and the cells deposited are used as the dendriticcell precursors.

This is followed by differentiating the dendritic cell precursors intoimmature or mature dendritic cells. AIM-V medium (Invitrogen) is used asa culture medium.

In addition to AIM-V medium, any commercially available medium used incell cultivation, such as RPMI-1640 Medium (Invitrogen), Dulbecco'sModified Eagle Medium (Invitrogen; hereinafter referred to as DMEM), TIL(Immuno-Biological Laboratories Co., Ltd.), epidermal keratinocytemedium (Kojin Bio, Ltd.; hereinafter referred to as KBM), and Iscove'sMedium (Invitrogen; hereinafter referred to as IMEM), may be used.Moreover, 5-20% bovine serum, fetal bovine serum (hereinafter referredto as FBS), human plasma or the like may be added as needed.

In the case of immature dendritic cells, they are obtained by adding adifferentiation-inducing factor to the culture medium and cultivatingthe dendritic cell precursors.

Any cytokine may be used as a differentiation-inducing factor; forexample, granulocyte-macrophage colony-stimulating factor (hereinafterreferred to as GM-CSF), interleukin-4 (hereinafter referred to as IL-4),stem cell factor (hereinafter referred to as SCF), IL-13, tumor necrosisfactor a (hereinafter referred to as TNF-α) and the like can efficientlyinduce the differentiation of immature dendritic cells. It is alsopreferable to add IL-1, IL-2, IL-3 and the like as needed. Morepreferably, the use of a combination of GM-CSF and IL-4 enablesefficient induction.

The cultivation is carried out under the conditions of 34-38° C., morepreferably 37° C., and 2-10% CO₂, more preferably 5% CO₂; thecultivation duration is preferably 5-7 days.

In the case of obtaining mature dendritic cells, an additionaldifferentiation-inducing factor is added on the 5th-7th day afterstarting the culture for further cultivation.

Any cytokine may be used as a differentiation-inducing factor; it ispreferable to use, for example, GM-CSF, IL-4, SCF, IL-1β, IL-6, IL-13,INF-α, prostaglandin E₂ (hereinafter referred to as PGE₂) and the liketo efficiently induce the differentiation of mature dendritic cells.IL-1, IL-2, IL-3 and the like are preferably added as needed. Morepreferably, employing a combination of GM-CSF, IL-4, IL-6, IL-1β, PGE₂and TNF-α enables efficient induction.

The cultivation is carried out under the conditions of 34-38° C., morepreferably 37° C., and 2-10% CO₂, more preferably 5% CO₂; the durationis preferably 24-48 hours.

Moreover, a method for obtaining immature or mature dendritic cells bycollecting hematopoietic stem cells (CD34-positive cells) as dendriticcell precursors and adding GM-CSF and TNF-α, as well as flt-3 Ligand(FL), c-kit Ligand (SCF) or trombopoetin (TPO), singly or incombination, or a method of directly collecting dendritic cell fractionsfrom blood or separated peripheral blood monocytes by using adensity-gradient medium such as Percoll, may also be used.

To the immature or mature dendritic cells obtained, a bisphosphonate isadded and cultured to prepare stimulating cells (dendritic cells pulsedwith a bisphosphonate). The concentration of the bisphosphonate added ispreferably 0.1-30 μM, more preferably 1-10 μM.

The duration of pulsing the cells with the bisphosphonate is preferably1 36 hours, more preferably 12 hours.

Since the dendritic cells obtained in this manner have the ability toactivate and/or proliferate γδ T-cells, they can be used as apharmaceutical composition capable of activating and/or proliferating γδT-cells either in vitro or in vivo. When used in vitro, they can be usedas a composition capable of activating and/or proliferating γδ T-cells.When used in vivo, they can be used as a dendritic cell vaccine capableof activating and/or proliferating γδ T-cells after rinsing and removingfree bisphosphonate. In either case, in vitro or in vivo, a cytokine(for example, IL-2), a protein (for example, albumin) or the like may beadded as needed.

Second Embodiment Pharmaceutical Composition Comprising the DendriticCells

The therapeutic method utilizing the dendritic cells of the applicationwill be explained below.

The dendritic cells obtained in the first embodiment are collected bycentrifugation or the like.

The collected cells are washed. Any washing solution may be used as longas it is isosmotic and suitable for use as a pharmaceutical composition.Considering the subsequent administration to a patient, the use ofphysiological saline, PBS or the like is preferable.

When suspended in physiological saline, the dendritic cells collectedbecome usable as a pharmaceutical preparation for administration. Inaddition, a cytokine may be added as needed.

The number of cells administered can be properly selected in accordancewith the condition of the patient; normally, however, the number ofcells is preferably 10⁶-10¹²/person, more preferably at least10⁷/person.

The preparation can be administered by intravenous, intradermal orhypodermic injection, injected into an affiliated lymph node, directlyinjected into a lesion, or drip-fed for general administration. It isalso possible to inject the preparation into an artery in the vicinityof a lesion.

By administering the dendritic cells of the present application in thismanner, the γδ T-cells in the patient's body can be activated. Since γδT-cells have nonspecific cytotoxic activity, they can be used in varioustreatments, for example, treating cancers and infectious diseases. Onebenefit of using dendritic cells in the form of a vaccine is acircumvention of the problem caused by directly administering abisphosphonate. A bisphosphosphonate's reaction to γδ T-cells in thebody is weakened and dissipated as the number of administrationsincreases, making the bisphosphonate incapable of repeatedlyproliferating γδ T-cells. By pulsing dendritic cells with abisphosphonate for use as a vaccine prevents this from occurring.

Third Embodiment The γδ T-Cell Culture Method Using the Dendritic Cells

The γδ T-cell culture method of the application will be explained indetail below.

The dendritic cells obtained in the first embodiment and the respondingcells are disseminated in a culture container.

The responding cells here refers to a cell subset containing γδ T-cells;mononuclear cells derived from peripheral blood and the like arepreferable.

There is no particular limitation for the container used; a plate,laboratory dish, flask, bag or the like normally employed in cultivationin the art may be used. The concentration of the individual cell subsetsdisseminated may be freely set in accordance with the situation.

AIM-V medium is used to culture the dendritic cells and the respondingcells. In addition to AIM-V medium, any commercially available culturemedium used in cell cultivation, such as RPMI-1640 medium, DMEM, TIL,KBM, and IMEM, may be used. Moreover, 5-20% bovine serum, FBS, humanplasma, cytokine or the like may be added as needed.

The cultivation is carried out under the conditions of 34-38° C., morepreferably 37° C., and 2-10% CO₂, more preferably 5% CO₂; thecultivation duration is preferably 5-8 days, more preferably 7 days.

The numbers of dendritic and responding cells disseminated can be setdepending on the container used and the purpose of the application. Themixing proportions of the dendritic and responding cells can be properlyset in accordance with the situation; considering the purpose, which isto increase the proportion of γδ T-cells in the reacted cells, thenumber of dendritic cells is preferably set smaller than the respondingcells.

The present application enables the collection of a cell populationcontaining activated γδ T-cells of high purity, in mass quantity and ina simple manner, without having to follow the complicated selection andpurification processes which were required by prior art techniques toobtain γδ T-cells. Moreover, the cell population obtained in this mannercan be used as it is in immune cell therapies. When the activated γδT-cells are used in such immune cell therapies, high levels oftherapeutic effect against tumors and infectious diseases are expected.

One benefit of activating and/or proliferating γδ T-cells in vitro is acircumvention of the problem associated with directly administering abisphosphonate, whose reaction to γδ T-cells in the body weakens anddissipates when the number of administrations increases so that it isincapable of repeatedly proliferating γδ T-cells. Activating and/orproliferating γδ T-cells in vitro for administration can prevent thisfrom occurring.

Fourth Embodiment Pharmaceutical Composition Comprising the γδ T-CellsObtained by the Present Method

The method of administering the γδ T-cells obtained above to a patientwill be explained next.

The γδ T-cells obtained by the method described in the third embodimentare collected by centrifugation and the like.

The cells collected are washed. Any washing solution may be used as longas it is isosmotic and suitable for use as a pharmaceutical preparation;considering the subsequent administration to a patient, the use ofphysiological saline, PBS or the like is preferable.

When suspended in physiological saline, the γδ T-cells collected becomeusable as a preparation for administration. In addition, a cytokine maybe added as needed.

The number of cells administered can be properly selected in accordancewith the condition of the patient; normally, however, the number ofcells is preferably 10⁸-10¹²/person, more preferably at least10⁹/person.

It can be administered by intravenous, intradermal or hypodermicinjection, injected into an affiliated lymph node, directly injectedinto a lesion, or drip-fed for general administration. The preparationcan also be injected into an artery in the vicinity of a lesion.

EXAMPLES

The present invention will be illustrated in more detail with referenceto examples; the present invention, however, is obviously not limited tothese examples.

Example 1 Collection and Preparation of Dendritic Cells

From the 30 ml of peripheral blood collected from a healthy donormononuclear cells were collected using a density gradient medium forseparating blood cells. The cells collected were washed several times toremove platelets and the like, and CD14-positive cells were isolatedusing MACS.

The dendritic cell precursors obtained were differentiated intodendritic cells. AIM-V medium with 10% FBS added thereto was used as aculture medium. To the medium 500 U/mL of GM-CSF (IMMUNEX) and 500 mL ofIL-4 (Osteogenetics GmbH) were added. Immature dendritic cells wereobtained in 5-7 days after starting the culture. Moreover, on the 5^(th)-7^(th) day after starting the culture, 100U/mL of IL-6 (R& DSystems), 10 ng/mL of IL-1β (CHEMICON), 10 ng/mL of TNF-α (PHARMINGEN),and 1 μg/ml of PGE₂ (SIGMA) were added for further cultivation. Maturedendritic cells were collected 24-48 hours later.

Example 2 Confirmation of the Condition of the Dendritic Cells

The antigens on the surface of the dendritic cells prepared weredetected using a flow cytometer (Epics XL-MCL, Beckman Coulter). To thecells to be measured, suspended in PBS, target antibodies were added andstained for 15 minutes at 4° C. in a shaded condition. The antibodiesused are PE-labeled anti-CD14, anti-CD83 and anti-HLA-DR antibodies(Beckman Coulter). As negative controls, the isotypes of the respectiveantibodies were used. The stained cells were washed with PBS andmeasured by using the Epics XL-MCL.

The results showed that the cells cultured with GM-CSF and IL-4 wereCD14 and CD83 negative, HLA-DR positive, and confirmed to be an immaturedendritic cell population. The cells cultivated with GM-CSF, IL-4, IL-6,IL-1β, TNFα, and PGE₂ were positive except for CD14, and confirmed to bea mature dendritic cell population.

Example 3 Proliferation of γδ T-cell With Dendritic Cells

To the suspensions containing the immature or mature dendritic cellsderived from peripheral blood prepared in Example 1, bisphosphonates,Aredia, Onclast and Zometa, were added to achieve the concentrations of10 μM, 10 μM and 1 μM, respectively, and cultured for about 12 hours toprepare stimulating cells (dendritic cells pulsed with bisphosphonates).As a negative control, dendritic cells cultured without adding abisphosphonate were used.

These stimulating cells, 5×10⁵ each, were respectively cultivated inmixed cultures of 2×10⁶ reacted cells using a 24-well plate (SUMILON) toa total volume of 1 mL (the ratio of reacted cells to stimulating cellswas 4 to 1). The cells remaining after isolating the CD14-positive cellsin Example 1 (CD14-negative cell population, mainly T-cell population),which had been suspended in AIM-V medium containing 10% FBS and 10%dimethyl sulfoxide (DMSO), frozen and stored, were used as the reactedcells after thawing and rinsing. The cultivation was carried out underthe conditions of about 37° C. and 5% CO₂ for 7 days.

An even better cell proliferation was observed in this mixed culturesolution when 50 U/mL of IL-2 was added. When the rate of cellproliferation was high, 100 U/mL of IL-2 and 1 mL of AIM-V mediumcontaining 10% FBS were added on the 4^(th)-6^(th) day.

Seven days later the number of cells was measured using a hemocytometer,and the proportion of γδ T-cells using a flow cytometer. For theantibodies, PC5-labeled anti-CD3 and FITC-labeled anti-pan γ/δantibodies (Beckman Coulter) were used. These antibodies were added tothe cells that were cultured and washed with PBS for dying at 4° C. for15 minutes in a shaded condition. The isotype of anti-pan γ/δ antibodywas utilized as a negative control.

As shown in FIG. 1, it was found that, compared to the controls(dendritic cells not pulsed with bisphosphonate), all of the maturedendritic cells and immature dendritic cells pulsed with Aredia,Onclast, and Zometa increased the proportion of γδT-cells in thecocultivated cell subsets.

Moreover, it was found that the immature cells pulsed withbisphosphonates increased the proportion of γδ T-cells more than themature dendritic cells pulsed with bisphosphonates did.

Example 4 Collection and Preparation of γδ T-Cells

From a healthy donor 30 ml of peripheral blood was collected, andperipheral blood mononuclear cells were collected using a densitygradient medium for blood cell separation. The cells collected werewashed several times to remove platelets and the like.

The peripheral blood monocytes obtained were suspended in AIM-V medium(10% FCS), and Aredia was added so that the concentration in theperipheral blood monocyte suspension was 10 μM.

This was cultivated for 14 days. During this period, AIM-V (10% FCS)medium and IL-2, at a final concentration of 1,000 U/ml, were added inaccordance with the cell proliferation.

Using a flow cytometer, the phenotype of the cells cultured wasconfirmed to be a cell subset containing at least 95% of γδ T-cells.

Example 5 Confirmation of the Activation of γδ T-Cells

In each well of a MultiScreen plate (Millipore), 70% ethanol was addedand removed within two minutes.

Each well of the plate was washed with 200 μl of PBS five times.

An anti-interferon(IFN)-γ antibody for coating (clone: 1-D1K, MABTECHELISpot for Human Interferon-γ kit) was diluted with PBS to 15 μg/ml,and added 100 μl/well.

The plate was left standing at 4° C. overnight.

The plate was washed with 200 μl/well of PBS four times.

AIM-V medium containing 10% FBS was added 200 μl/well, and blocking wasperformed at room temperature for at least 30 minutes.

The blocking medium was removed and the plate was washed with 200μl/well of PBS four times.

The γδ T-cells obtained in Example 4 were collected by centrifugationand washed twice with AIM-V.

To 30,000 of the γδ T-cells collected, and 15,000 of the immature ormature dendritic cells obtained in Example 1 Aredia, prepared to have afinal concentration of 10 μM, was added, and precultivated in a 15 mltube (Falcon) under the conditions of 37° C. and 5% CO₂ for two hours.At the same time, precultivation of γδ T-cells by themselves,precultivation of γδ T-cells with only Aredia added thereto, andprecultivation of the respective dendritic cells by themselves were alsoconducted. Each culture volume was adjusted to 300 μl.

The plate was washed with PBS after blocking, and each group of cellswhich completed precultivation under the respective conditions wasdisseminated in three wells, 100 μl/well.

They were cultured overnight under the conditions of 37° C. and 5% CO₂.

The culture solution containing the cells was removed and the plate waswashed five times with 200 μl/well of PBS.

Biotin-labeled anti-IFN-γ antibody for detection (clone: 7-B6-1, MABTECHELISpot for Human Interferon-γ kit) was diluted to 1 μg/ml with PBScontaining 0.5% FBS and added 100 μl/well.

The plate was left standing for two hours at room temperature.

The PBS containing Biotin-labeled anti-IFN-γ antibody was removed, andthe plate was washed five times with 200 μl/well of PBS.

Alkaliphosphatase-bonded streptoabizine (MABTECH ELISpot for HumanInterferon-γ kit) was diluted with PBS containing 0.5% FBS to 1:1000,and added 100 μl/well.

The plate was left standing for one hour at room temperature.

The plate was washed five times with 200 μl/well of PBS.

BCIP/NBTplus substrate stock solution (Wako) was added 100 μl/well; theplate was left standing in the dark until spots were recognizable.

When spots were visually recognized, the plate was washed thoroughlywith distilled water.

After confirming that the membrane on the plate was dry, the number ofspots was measured using an ELISpot reader (AID Autoimmune DiagnostikaGmbH), and the data was analyzed using the AID software version 3.1(AID).

The results showed that the number of spots and the spot intensityincreased only when the dendritic cells and Aredia were addedsimultaneously to the γδ T-cells. The results also showed that theimmature dendritic cells pulsed with the bisphosphonate stimulated thegeneration of IFN-γ more than the mature dendritic cells did.

Potential for Industrial Application

As described above, the dendritic cells pulsed with bisphosphonates asdescribed in the present application are capable of selectivelyactivating and/or proliferating the γδ T-cells contained in peripheralblood. Accordingly, they can be used as a composition capable ofactivating and/or proliferating γδ T-cells in vitro. Moreover, byadministering them to a patient as an administrable composition, γδT-cells can be activated in vivo, from which effective treatment ofcancers and viral infections can be expected.

1. A therapeutic method wherein cultured, isolated dendritic cells whichhave been pulsed with a bisphosphonate-based bone metabolism improvingdrug in vitro, are administered to a patient in an amount effective fortreating a cancer and/or an infectious disease.
 2. The therapeuticmethod of claim 1, wherein said cultured, isolated dendritie cells haveenhanced functional activity for activating and/or proliferating γδT-cells in culture in relation to cultured, isolated dendritic cellswhich have not been exposed to a bisphosphonate-based bone metabolismimproving drug.
 3. The therapeutic method of claim 1, wherein saidcultured, isolated dendritic cells are immature dendritic cells.
 4. Thetherapeutic method of claim 1, wherein said cultured, isolated dendriticcells are a mixture of immature and mature dendrite cells.
 5. Thetherapeutic method of claim 1, wherein said bisphosphonate-based bonemetabolism improving drug is selected from the group consistingpamidronic acid, alendronic acid, zoledronic acid, risedronic acid,ibandronic acid, incadronic acid, etidronic acid, their salts theirhydrates and combinations thereof.
 6. The therapeutic method of claim 1,wherein said cultured, isolated dendritic cells are produced by aprocess comprising: a) differentiating precursor cells in vitro, whereinthe precursor cells are selected from the group consisting (i) isolatedCD14 positive cells; (ii) isolated peripheral blood mononuclear cells;(iii) isolated CD34 positive hematopoietic stem cells; and (iv) amixture thereof, to provide isolated, cultured dendritic cells; and b)pulsing the cultured isolated dendritic cells with saidbisphosphonate-based bone metabolism improving drug.
 7. The therapeuticmethod of claim 6 wherein said precursor cells are derived from saidpatient.
 8. The therapeutic method of claim 2 wherein said cultured,isolated dendritic cells comprise immature dendritic cells.
 9. Themethod of claim 8, wherein the bisphosphonate-based bone metabolismimproving drug is pamidronic acid, a salt thereof, a hydrate thereof, ora mixture thereof.
 10. The method of claim 8, wherein thebisphosphonate-based bone metabolism improving drug is alendronic acid,a salt thereof, a hydrate thereof, or a mixture thereof.
 11. The methodof claim 8, wherein the bisphosphonate-based bone metabolism improvingdrug is zoledronic acid, a salt thereof, a hydrate thereof, or a mixturethereof.
 12. The therapeutic method of claim 2 wherein said cultured,isolated dendritic cells are administered to the patient in an amounteffective for treating a cancer.
 13. The therapeutic method of claim 2wherein said cultured, isolated dendritic cells are administered to thepatient in an amount effective for treating an infectious disease. 14.The therapeutic method of claim 2 wherein said infectious disease is abacterial infection.